ClinVar Miner

Submissions for variant NM_015850.4(FGFR1):c.1962G>C (p.Lys654Asn) (rs1057519897)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000422833 SCV000506354 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433539 SCV000506355 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444182 SCV000506356 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426798 SCV000506357 likely pathogenic Lymphoblastic leukemia, acute, with lymphomatous features 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000437662 SCV000506358 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443011 SCV000506359 likely pathogenic Astrocytoma 2016-05-31 no assertion criteria provided literature only

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